Canonical Allele Identifier: CA2336427471

Gene: B9D2 TMEM91

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41355261T= , CM000681.2:g.41355261T=	GRCh38
NC_000019.9:g.41861166T= , CM000681.1:g.41861166T=	GRCh37
NC_000019.8:g.46553006T=	NCBI36
NG_013091.1:g.13913A=
NG_013364.1:g.3666A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243578.8:c.215-248A= (B9D2) MANE Select	ENSP00000243578.2:n.215-248A=
ENST00000675972.1:c.215-248A= (B9D2)	ENSP00000501911.1:n.215-248A=
ENST00000243578.7:c.215-248A= (B9D2)	ENSP00000243578.2:n.215-248A=
ENST00000539627.5:c.-30+4059T= (TMEM91)	ENSP00000441900.1:n.-30+4059T=
ENST00000594416.1:c.*61-248A= (B9D2)	ENSP00000469666.1:n.*61-248A=
ENST00000604123.5:c.142+946T= (TMEM91)	ENSP00000474871.1:n.142+946T=
ENST00000604424.1:n.350+4059T=
NM_030578.3:c.215-248A= (B9D2)	NP_085055.2:n.215-248A=
XM_006723405.1:c.89-248A= (B9D2)	XP_006723468.1:n.89-248A=
XM_011527349.1:c.215-248A= (B9D2)	XP_011525651.1:n.215-248A=
XM_011527350.1:c.56-248A= (B9D2)	XP_011525652.1:n.56-248A=
XM_011527349.2:c.215-248A= (B9D2)	XP_011525651.1:n.215-248A=
XM_011527350.2:c.56-248A= (B9D2)	XP_011525652.1:n.56-248A=
NM_030578.4:c.215-248A= (B9D2) MANE Select	NP_085055.2:n.215-248A=